Red-green colour blindness is an X-linked recessive trait. This means the gene responsible is on the X chromosome. Females (XX) must inherit two copies of the recessive allele (XcXc) to be affected, while males (XY) only need one (XcY).
We determine the genotypes based on the information given:
The genetic cross is between the mother (XCXc) and the father (XcY). We can use a Punnett square to visualize the possible offspring genotypes:
| Mother's Gametes | |||
| XC | Xc | ||
| Father's Gametes | Xc | XCXc (Daughter, normal phenotype) | XcXc (Daughter, colour-blind phenotype) |
| Y | XCY (Son, normal phenotype) | XcY (Son, colour-blind phenotype) | |
We need the probability of a colour-blind daughter. A colour-blind daughter has the genotype XcXc.
The probability of having a colour-blind daughter is 50%.
The allele associated with albinism in humans is recessive ($c$). The probability that an albino male ($cc$) and a carrier female ($Cc$) will have an offspring with normal skin pigmentation is _________.
(Round off to one decimal place)